期刊
DRUG DELIVERY
卷 15, 期 5, 页码 267-275出版社
TAYLOR & FRANCIS LTD
DOI: 10.1080/10717540802174662
关键词
etoposide; nanoparticles; nanoprecipitation
Etoposide-loaded nanoparticles were prepared using nanoprecipitation and emulsion solvent evaporation techniques using polylactide-co-glycolic acid and poly(epsilon-caprolactone) in presence of Pluronic F68, respectively. Effect of formulation variables like stabilizer concentration, amount of polymer, and drug was studied. These parameters were found to affect particle size, zeta potential, drug content, and entrapment efficiency of nanoparticles. The methods produced nanoparticles with good entrapment efficiency of around 80%. Recovery of nanoparticles was as high as 95% and drug content was around 1.5%. Increase in lactide content decreased the release of etoposide in vitro and poly(epsilon-caprolactone) nanoparticles retarded etoposide release for 48 hr. The results show the suitability of polylactide-co-glycolic acid and poly(epsilon-caprolactone) nanoparticles as potential carriers for controlled delivery of etoposide.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据